NDC11 68084085033
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 68084-0850-33 | 68084-0850 |
| 68084-850-33 | 68084-850 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Potassium Citrate | POTASSIUM CITRATE | American Health Packaging | 1201c777-2388-4235-bb8f-eb7dc1e867f8 | 2024-09-03 | Warnings, Adverse reactions | 68084-850-33 68084-850 68084085033 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.